US2948592A - Process for producing pure boric acid and potassium sulfate - Google Patents
Process for producing pure boric acid and potassium sulfate Download PDFInfo
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- US2948592A US2948592A US793630A US79363059A US2948592A US 2948592 A US2948592 A US 2948592A US 793630 A US793630 A US 793630A US 79363059 A US79363059 A US 79363059A US 2948592 A US2948592 A US 2948592A
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- boric acid
- potassium sulfate
- temperature
- potassium
- aqueous solution
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- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 title claims description 61
- 239000004327 boric acid Substances 0.000 title claims description 56
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 title claims description 46
- 229910052939 potassium sulfate Inorganic materials 0.000 title claims description 46
- 235000011151 potassium sulphates Nutrition 0.000 title claims description 45
- 238000000034 method Methods 0.000 title claims description 37
- 229910001868 water Inorganic materials 0.000 claims description 19
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 17
- 239000000243 solution Substances 0.000 claims description 15
- 239000007864 aqueous solution Substances 0.000 claims description 12
- 239000012452 mother liquor Substances 0.000 claims description 12
- 238000006243 chemical reaction Methods 0.000 claims description 11
- 239000013078 crystal Substances 0.000 claims description 9
- WUUHFRRPHJEEKV-UHFFFAOYSA-N tripotassium borate Chemical compound [K+].[K+].[K+].[O-]B([O-])[O-] WUUHFRRPHJEEKV-UHFFFAOYSA-N 0.000 claims description 7
- 238000001816 cooling Methods 0.000 claims description 6
- 238000010438 heat treatment Methods 0.000 claims description 5
- 238000004064 recycling Methods 0.000 claims description 4
- 238000000926 separation method Methods 0.000 claims description 4
- 230000001376 precipitating effect Effects 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- UCQWTMHYSWMPFM-UHFFFAOYSA-L dipotassium boric acid sulfate Chemical compound S(=O)(=O)([O-])[O-].[K+].B(O)(O)O.[K+] UCQWTMHYSWMPFM-UHFFFAOYSA-L 0.000 claims 1
- 239000000706 filtrate Substances 0.000 description 20
- 239000007787 solid Substances 0.000 description 13
- 239000000203 mixture Substances 0.000 description 10
- PYUBPZNJWXUSID-UHFFFAOYSA-N pentadecapotassium;pentaborate Chemical compound [K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[O-]B([O-])[O-].[O-]B([O-])[O-].[O-]B([O-])[O-].[O-]B([O-])[O-].[O-]B([O-])[O-] PYUBPZNJWXUSID-UHFFFAOYSA-N 0.000 description 7
- 239000002994 raw material Substances 0.000 description 7
- 238000010790 dilution Methods 0.000 description 5
- 239000012895 dilution Substances 0.000 description 5
- 239000002002 slurry Substances 0.000 description 5
- 238000002425 crystallisation Methods 0.000 description 4
- 230000008025 crystallization Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 229920006395 saturated elastomer Polymers 0.000 description 4
- 125000004122 cyclic group Chemical group 0.000 description 3
- 239000002253 acid Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- 101100165918 Caenorhabditis elegans cam-1 gene Proteins 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- FZQSLXQPHPOTHG-UHFFFAOYSA-N [K+].[K+].O1B([O-])OB2OB([O-])OB1O2 Chemical compound [K+].[K+].O1B([O-])OB2OB([O-])OB1O2 FZQSLXQPHPOTHG-UHFFFAOYSA-N 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229940072033 potash Drugs 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 238000010591 solubility diagram Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B35/00—Boron; Compounds thereof
- C01B35/06—Boron halogen compounds
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B35/00—Boron; Compounds thereof
- C01B35/08—Compounds containing boron and nitrogen, phosphorus, oxygen, sulfur, selenium or tellurium
- C01B35/10—Compounds containing boron and oxygen
-
- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01D—COMPOUNDS OF ALKALI METALS, i.e. LITHIUM, SODIUM, POTASSIUM, RUBIDIUM, CAESIUM, OR FRANCIUM
- C01D5/00—Sulfates or sulfites of sodium, potassium or alkali metals in general
- C01D5/02—Preparation of sulfates from alkali metal salts and sulfuric acid or bisulfates; Preparation of bisulfates
Definitions
- the general object of the present invention is to provide a process for producing pure boric acid and potassium sulfate from a potassium borate and sulfuric acid in a continuous, cyclic operation. More specifically, the object of this invention is to provide a process for the use of potassium pentaborate as an economic 'raw material for the above process.
- the general advantage of using a potassium borateas raw material is the relatively greater value of the potassium sulfate produced, as compared to the sodium sulfate by-product produced when a sodium borate is used as a raw material.
- the particular advantage of using potassium pentaborate is due to the considerably greater yield of boric acid obtained per unit of sulfuric acid required.
- Potassium pentaborate can readily be prepared as a relatively cheap material, for example as described in my Patent No. 2,395,566 or as an intermediate, as shown in my Patent No. 2,3955 64, and can therefore be considered as a readily available raw material for the present process.
- States Patent Figure 1 is a graphical representation of the cyclic process of this invention using a preferred set of temperature conditions.
- Figure 2 is a graphical representation of two additional cyclic processes using temperature conditions differing I Figure 1 where the sequence of operations is shown graphically starting with point A and following the arrows through successive points to E and back to point A to complete the cycle.
- FIG. 1 The process of Figure 1 is based upon starting with a 35 C. boric acid filtrate having the composition of point A on the diagram. This liquor serves as feed to an evaporator where it is concentrated from point A along a line (labeled Concentrat-ion) through the zero axis to point B.- The concentrated liquor is next cooled to 75 C. to crystallize a crop of K SO and yield a mother liquor of the'composition represented by point C. The potassium sulfate solids are separated and the mother liquor is next diluted with water to a point along the line from point C extended through the zero axis to point D.
- a line labeled Concentrat-ion
- the concentrated liquor is next cooled to 75 C. to crystallize a crop of K SO and yield a mother liquor of the'composition represented by point C.
- the potassium sulfate solids are separated and the mother liquor is next diluted with water to a point along the line from point C extended through the zero axis to point D.
- a quantity of boric acid filtrate (4300 gms.) was combined with the cake wash (550 gms.) and then concentrated by evaporation at atmospheric pressure. About 2480 grams of water were removed. The agitated concentrated liquor was then cooled to about C.
- the hot concentrated liquor (76 C.) was decanted from the K 80 solids and saved for recycling purposes.
- the potassium sulfate solids were then agitated in about 7 500 cc. of boric acid filtrate maintained at about 35 C.
- the solids were then centrifuged and washed with water saturated with K 80 at 35' C. The washed wet solids were dried .at C.
- Figure 2 relates to two additional runs using temperatures which vary considerably from these described in the example above.
- a particular cycle may be set up,rthe most direct is to set the boric acid crystallizer temperature and the boric acid slurry concentration. After these factors have been set, the solubilities of the I system establishthe complete cycle.
- the amount of water added as dilution in the equilibrium cycle was equal to that evaporated exclusive of that required by the equation set out at the beginning of the specification less the dilution from cakewash, etc.
- the corrected dilution is adjusted to yield a boric acid filtrate slightly under saturated with respect to potassium sulfate.
- the concentration percycle was based upon the composition of the K 80 filtrate as determined by extending a line on the graph of Figure 2 through the diluted filtrate composition and the zero axis to the intersection of the solubility curve.
- the composition of this point in grams/ 100 grams H O is as follows; representing saturation at approximately 76 C.
- This slurry is filtered and the filtrate is diluted with 78.89 units of Water and a second cycle is carried out by adding reaction materials to the diluted liquor as before.
- the boric acid crystallizer can be operated somewhat below and somewhat above the 15 C. actually shown on the examples.
- the potassium sulfate crystallizer may be operated somewhat below the 75 C. shown in the example and somewhat above the 85 C. shown.
- the range of between about 70 C. and somewhat in excess of about 95 C. are suitable, although a temperature approaching 100 C. is difficult to handle (at atmospheric pressure) for obvious reasons. However, theoretically there is no reason why a temperature approaching 100 C. might not be used.
- variations from the temperatures are possible with results only somewhat impaired from those disclosed here. The process is limited only by economic factors, e.g., the relative cost of heating and cooling as against the yield obtained.
- the improvements comprising: heating the mother liquor remaining after the separation therefrom of said boric acid crystals to a temperature in excess of about 75 C. to evaporate at least about one-half of said water therefrom to exceed the solubility of said potassium sulfate 7 with respect to said liquor at a temperature of about 75 C.; thereafter cooling said mother liquor to about said C.
- the improvements comprising: heating the mother liquor remaining after the separation therefrom of said boric acid crystals to a temperature in excess of a predetermined temperature of between about 70 C. and 95 C. to evaporate at least about one-half of said water therefrom to exceed the solubility of said potassium sulfate with respect to said liquor at said predetermined temperature of between about 70 C. and 95 C.; thereafter cooling said mother liquor to said predetermined temperature of between about 70 C. and 95 C.
Description
Aug. 9, 1960 F. H. MAY 2,943,592
. PROCESS FOR PRODUCING PURE BORIC ACID AND POTASSIUM SULFATE Fixed Feb. 16,. 1959 2 Sheets-Sheet 1 SOLUBILITY SY5TEM= K so n sog-u o ask-75m. I
SAT- BOTH PHASES- 6m. H 6m. H O
INVENTOR. Frank H. May
ECKHOFF SLICK TORNEYS M KZ- a)" A M50158 0'' THE (IR Aug. 9,
Filed Feb. 16, 1959 1960 F. H. MAY 2,948,592 PROCESS FOR PRODUCING PURE BORIC ACID AND POTASSIUM SULFATE 2 Sheets-Sheet 2 SOLUBILITY SYSTEM! K SO H 80 H O g CRYSTALLIZATION (K 50 6o AEUR E J WITH K350 a O: z g1)/O so E' 40 A k 00 I o (J (J a a 2 e v 0* m I N i C 5 2oam CRYSTALLIZATION (H3803) 2 1 IO N 9 zh -'Ex. I1 76C CYCLE .,,--EX. 1:: 45-s5c CYCLE O l I l, 0 IO 20 so 7o Gm. H3BOS/IOO cam-1 o INVENTOR. FRANK H. MAY
ygMeg/ gr THE FIRM PROCESS FOR PRODUCING PURE BORIC ACID AND POTASSIUM SULFATE Frank H. May, Whittier, Calif., assignor to American Potash & Chemical Corporation, a corporation of Delaware Filed Feb. 16, 1959, Ser. No. 793,630
6 Claims. (Cl. 23-149) The general object of the present invention is to provide a process for producing pure boric acid and potassium sulfate from a potassium borate and sulfuric acid in a continuous, cyclic operation. More specifically, the object of this invention is to provide a process for the use of potassium pentaborate as an economic 'raw material for the above process.
The general advantage of using a potassium borateas raw material is the relatively greater value of the potassium sulfate produced, as compared to the sodium sulfate by-product produced when a sodium borate is used as a raw material. The particular advantage of using potassium pentaborate is due to the considerably greater yield of boric acid obtained per unit of sulfuric acid required.
Potassium pentaborate can readily be prepared as a relatively cheap material, for example as described in my Patent No. 2,395,566 or as an intermediate, as shown in my Patent No. 2,3955 64, and can therefore be considered as a readily available raw material for the present process.
So far as the available literature is'concerned, there is no published information describing a process for producing potassium sulfate and boric acid from potassium borates and sulfuric acid. Solubilities in the system K SO H BO H O do not permit establishment of a simple heating and cooling cycle for the alternate separation of boric acid and potassium sulfate.
In the drawings:
States Patent Figure 1 is a graphical representation of the cyclic process of this invention using a preferred set of temperature conditions.
Figure 2 is a graphical representation of two additional cyclic processes using temperature conditions differing I Figure 1 where the sequence of operations is shown graphically starting with point A and following the arrows through successive points to E and back to point A to complete the cycle.
The process of Figure 1 is based upon starting with a 35 C. boric acid filtrate having the composition of point A on the diagram. This liquor serves as feed to an evaporator where it is concentrated from point A along a line (labeled Concentrat-ion) through the zero axis to point B.- The concentrated liquor is next cooled to 75 C. to crystallize a crop of K SO and yield a mother liquor of the'composition represented by point C. The potassium sulfate solids are separated and the mother liquor is next diluted with water to a point along the line from point C extended through the zero axis to point D. Controlled amounts of K B O -8H O and Patented Au 9, i980 ice sulfuric acid in stoiohiometric quantities are then added to this diluted liquor to produce a liquor of composition E. This reaction solution is then cooled to 35 C. to crystallize a crop of boric .acid and produce a mother liquor having the composition of point A; the starting point for the process. The boric acid solids are separated by filtering and the filtrate sent to the evaporator.
The following is ofliered as a specific example of the method of this invention, it being understood that this example is to be construed as illustrative only:
EXAMPLE I To a solution of 451 grams of K 80 and 408 grams of H BO in 3542 grams H 0, 770 grams of Gms. salt/100 g. H O K SO 20.01
H BO product Wt. percent H- BO 99.7 Nil S0 Trace H O (diff) 0.3
A quantity of boric acid filtrate (4300 gms.) was combined with the cake wash (550 gms.) and then concentrated by evaporation at atmospheric pressure. About 2480 grams of water were removed. The agitated concentrated liquor was then cooled to about C. A
plugpipette sample of clear filtrate was taken at 76 C. V
and the following analysis was obtained:
76 C. K 50 crystallizer liquor (point C) Gms. salt/100 g. H O K SO 36.6. H BO 35.7
The hot concentrated liquor (76 C.) was decanted from the K 80 solids and saved for recycling purposes.
The potassium sulfate solids were then agitated in about 7 500 cc. of boric acid filtrate maintained at about 35 C. The solids were then centrifuged and washed with water saturated with K 80 at 35' C. The washed wet solids were dried .at C.
Analysis of dry K 80 solids Wt. percent- K2804 99.95 H3BO3 0.05
As aforestated, Figure 2 relates to two additional runs using temperatures which vary considerably from these described in the example above. Although there are several ways in which a particular cycle may be set up,rthe most direct is to set the boric acid crystallizer temperature and the boric acid slurry concentration. After these factors have been set, the solubilities of the I system establishthe complete cycle. In the examples As in the example above, the amount of water added as dilution in the equilibrium cycle was equal to that evaporated exclusive of that required by the equation set out at the beginning of the specification less the dilution from cakewash, etc. The corrected dilution is adjusted to yield a boric acid filtrate slightly under saturated with respect to potassium sulfate. The concentration percycle was based upon the composition of the K 80 filtrate as determined by extending a line on the graph of Figure 2 through the diluted filtrate composition and the zero axis to the intersection of the solubility curve.
The two additional examples which follow, as well as that preceding example, are all based upon operation at points near saturation with respect to both potassium sulfate and boric acid. However, it is obvious that the process may be operated at points along an isotherm somewhat removed from saturation with respect to one phase without departing from the basic process. For example, by increasing the dilution and corresponding concentration, and with proper control of operating ternperatures, the process can be controlled to crystallize boric acid from a solution which is considerably undersaturated with respect to potassium sulfate and to crystallize potassium sulfate from a solution which is considerably undersaturated with respect to boric acid. However, the preferred process involves operating with saturated conditions and the two examples which follow are based upon operation of the crystallization steps of the process at points close to saturation with respect to the phase to be retained in solution in a manner similar to the process of Example 1.
EXAMPLE II Basis:
(1) Boric acid crystallization temperature=20 C.
(2) Boric acid crystallizer slurry to contain 24 grams H BO solids/ 100 grams H 0. (3) K B O -8H O borate raw material.
Composition of 20 C. liquor saturated with H BO and filtrate):
20 c. H3BO3 M.L.:
H BO 7.6.
20 C. H BO crystallizer slurry:
H BO 7.6+24 solids=3l.6 total.
Reaction materials required/24 units of H BO produced:
KzB 100 1031120 +HzS 04+6Hz0 K SO +1OHaB O a 22.8 3.81 4.20 6.76 24.0 The dilute K 80 filtrate (before addition of reaction materials).
K 80 l14.8-'6.76=8.04. H3BO3 o 100.0.
A straight line drawn through the plot of the diluted K 80 (filtrate and the zero axis on the solubility diagram crosses the solubility curve representing saturation with H BO and K 30 at a point corresponding approximately to the solution composition of the K 50 crystallizer. The composition of this point in grams/ 100 grams H O is as follows; representing saturation at approximately 76 C.
K2804 38.1 H3BO3 36.0 H2O 100.0
The concentrated liquor then, as derived from concentration of the boric acid filtrate, must contain (7.6/36.0) (100)=21.11 units of water or 100-2.1.11
=78.89 grams of water are evaporated for every 100 grams of water which Was present in the boric acid filtrate.
The concentrated liquor resulting from concentration of this amount of boric acid filtrate is equivalent to:
Cone. K280i Liquor Boric Acid Filtrate Weight Liq. Comp gar/100 gm. H 0
evap.
=3.29 units of water evaporated/unit of 11 1303 produced.
Cooling this liquor to 76 C. (approx) 76 C. K 50 crystallizer liquor WEIGHT Liq. Comp. Liq. Solids gin/100 gm. H20
This slurry is filtered and the filtrate is diluted with 78.89 units of Water and a second cycle is carried out by adding reaction materials to the diluted liquor as before.
EXAMPLE 1 11 In this example assume as a basis:
(1) Boric acid crystallizer temperature=45 C.
(2) Boric acid crystallizer slurry to contain 30 grams H BO solids/ 100 grams H O in boric acid filtrate.
(3) K B O -8H O raw material.
Following exactly the same procedure as in Example 11, the liquor compositions, reaction quantities of raw materials and evaporated water are as follows:
Boric acid crystallizer WEIGHT AND COIMPOSITION 45 o. Borlc Acid Filtrate Liq. Wt. & Comp. Solids 24.0 ICQSOLU 24.0 16.5 H3BO3 16.5 30.0 100.0 II20 100.0 140.5
Concentrated potassium sulfate liquor Weight Cornp Potassium sulfate crystallizer C. approx.)
\VEIGHT Liq. Solids Liq. Comp.
Dilute potassium sulfate filtrate WEIGHT AND COMP.
K580 15.55 H BO 16.5 0 100.0
H O evap.=65.84=2.2 units/unit of H BO =dilution water added to K SO filtrate.
K2B4O7 K2SO4+4H3BO3 In such a case, the only important difference in the overall process would be the ratios of K 80 and H BO produced. v
The examples preceding represent the preferred operating conditions, but a certain amount of variation from the temperature conditions described is possible. For example, the boric acid crystallizer can be operated somewhat below and somewhat above the 15 C. actually shown on the examples. The potassium sulfate crystallizer may be operated somewhat below the 75 C. shown in the example and somewhat above the 85 C. shown. The range of between about 70 C. and somewhat in excess of about 95 C. are suitable, although a temperature approaching 100 C. is difficult to handle (at atmospheric pressure) for obvious reasons. However, theoretically there is no reason why a temperature approaching 100 C. might not be used. Hence, in the claims which follow it is to be borne in mind that variations from the temperatures are possible with results only somewhat impaired from those disclosed here. The process is limited only by economic factors, e.g., the relative cost of heating and cooling as against the yield obtained.
Obviously many modifications and variations of the invention as hereinbefore set forth may be made without departing from the spirit and scope thereof, and therefore only such limitations should be imposed as are indicated in the appended claims.
This application is a continuation-in-part of my application Serial No. 631,858, filed December 31, 1956, for Process for Producing Pure Boric Acid and Potassium Sulfate, now abandoned.
I claim:
1. In a process for the preparation of boric acid wherein a potassium borate and sulfuric acid are added to a recycled aqueous solution containing dissolved boric acid and potassium sulfate and allowed to react to produce boric acid and potassium sulfate in quantities sufiicient to precipitate boric acid at a temperature of about 35 C. while substantially all of said potassium sulfate remains in solution and wherein said solution is heated to a temperature sufficiently in excess of said 35 C. to dissolve all of said potassium sulfate and said boric acid and said solution is thereafter adjusted to about said 35 C. temperature to precipitate a crop of boric acid crystals about equivalent to the quantity of boric acid introduced by said reaction without precipitating potassium sulfate and said boric acid is separated therefrom, the improvements comprising: heating the mother liquor remaining after the separation therefrom of said boric acid crystals to a temperature in excess of about 75 C. to evaporate at least about one-half of said water therefrom to exceed the solubility of said potassium sulfate 7 with respect to said liquor at a temperature of about 75 C.; thereafter cooling said mother liquor to about said C. temperature to precipitate a crop of potassium sulfate crystals about equivalent to the quantity of potassium sulfate introduced by said reaction; separating said potassium sulfate; thereafter adding water to said mother liquor in an amount suflicient to replace that lost during said process, wherein to form an aqueous solution of a volume substantially equal to the said recycled aqueous solution initially present; and recycling the aqueous solution so formed in said process.
2. The process of claim 1 wherein said potassium borate is potassium pentaborate and wherein said sulfuric acid and said potassium pentaborate are proportioned to provide stoichiometric quantities of each to satisfy the equation:
3. In a process for the preparation of boric acid wherein a potassium borate and sulfuric acid are added to a recycled aqueous solution containing dissolved boric acid and potassium sulfate and allowed to react to produce boric acid and potassium sulfate in quantities sufficient to precipitate boric acid at a predetermined temperature of between about 20 C. and 45 C. while substantially all of said potassium sulfate remains in solution and wherein said solution is heated to a temperature sufliciently in excess of said predetermined temperature of between about 20 C. and 45 C. to dissolve all of said potassium sulfate and said boric acid and said solution is thereafter adjusted to about said predetermined temperature of between about 20 C. and 45 C. to precipitate a crop of boric acid crystals about equivalent to the quantity of boric acid introduced by said reaction without precipitating potassium sulfate and said boric acid is separated therefrom, the improvements comprising: heating the mother liquor remaining after the separation therefrom of said boric acid crystals to a temperature in excess of a predetermined temperature of between about 70 C. and 95 C. to evaporate at least about one-half of said water therefrom to exceed the solubility of said potassium sulfate with respect to said liquor at said predetermined temperature of between about 70 C. and 95 C.; thereafter cooling said mother liquor to said predetermined temperature of between about 70 C. and 95 C. to precipitate a crop of potassium sulfate crystals about equivalent to the quantity of potassium sulfate introduced by said reaction; separating said potassium sulfate; thereafter adding water to said mother liquor in an amount sufiicient to replace that lost during said process, whereby to form an aqueous solution of a volume substantially equal to the said recycled aqueous solution initially present; and recycling the aqueous solution so formed in said process.
4. The process of claim 3 wherein said potassium borate is potassium pentaborate and wherein said sulfuric acid and said potassium pentaborate are proportioned to provide stoichiometric quantities of each to satisfy the equation:
5. The process of claim 3 wherein said first predetermined temperature is about 20 C. and wherein said second predetermined temperature is about 76 C.
6. The process of claim 3 wherein said first predetermined temperature is about 45 C. and said second predetermined temperature is about C.
References Cited in the file of this patent UNITED STATES PATENTS 1,888,391 Newman Nov. 22, 1932 2,014,009 Burke Jan. 4, 1938 2,637,626 Taylor May 5, 1953
Claims (1)
1. IN A PROCESS FOR THE PREPARATION OF BORIC ACID WHEREIN A POTASSIUM BORATE AND SULFURIC ACID ARE ADDED TO A RECYCLED AQUEOUS SOLUTION CONTAINING DISSOLVED BORIC ACID AND POTASSIUM SULFATE AND ALLOWED TO REACT TO PRODUCE BORIC ACID POTASSIUM SULFATE IN QUANTITIES SUFFICIENT TO PRECIPITATE BORIC ACID AT A TEMPERATURE OF ABOUT 35* C. WHILE SUBSTANTIALLY ALL OF SAID POTASSIUM SULFATE REMAINS IN SOLUTION AND WHEREIN SAID SOLUTION IS HEATED TO A TEMPERATURE SUFFICIENTLY IN EXCESS OF SAID35* C. TO DISSOLVE ALL OF SAID POTASSIUM SULFATE AND SAID BORIC ACID AND SAID SOLUTION IS THEREAFTER ADJUSTED TO ABOUT SAID 35*C. TEMPERATURE TO PRECIPITATE A CROP OF BORIC ACID CRYSTALS ABOUT EQUIVALENT TO THE QUANTITY OF BORIC ACID INTRODUCED BY SAID REACTION WITHOUT PRECIPITATING POTASSIUM SULFATE AND SAID BORIC ACID IS SEPARATED THEREFROM, THE IMPROVEMENTS COMPRISING: HEATING THE MOTHER LIQUOR REMAINING AFTER THE SEPARATION THEREFROM OF SAID BORIC ACID CRYSTALS TO A TEMPERATURE IN EXCESS OF ABOUT 75*C. TO EVAPORATE AT LEAST ABOUT ONE-HALF OF SAID WATER THEREFROM TO EXCEED THE SOLUBILITY OF SAID POTASSIUM SULFATE WITH RESPECT TO SAID LIQUOR AT A TEMPERATURE OF ABOUT 75*C. THEREAFTER COOLING SAID MOTHER LIQUOR TO ABOUT SAID 75*C. TEMPERATURE TO PRECIPITATE A CROP OF POTASSIUM SULFATE CRYSTALS ABOUT EQUIVALENT TO THE QUANTITY OF POTASSIUM SULFATE INTRODUCED BY SAID REACTION, SEPARATING SAID POTASSIUM SULFATE, THEREAFTER ADDING WATER TO SAID MOTHER LIQUOR IN AN AMOUNT SUFFICIENT TO REPLACE THAT LOST DURING SAID PROCESS, WHEREIN TO FORM AN AQUEOUS SOLUTION OF A VOLUME SUBSTANTIALLY EQUAL TO THE SAID RECYCLED AQUEOUS SOLUTION INITIALLY PRESENT, AND RECYCLING THE AQUEOUS SOLUTION SO FORMED IN SAID PROCESS.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US793630A US2948592A (en) | 1959-02-16 | 1959-02-16 | Process for producing pure boric acid and potassium sulfate |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US793630A US2948592A (en) | 1959-02-16 | 1959-02-16 | Process for producing pure boric acid and potassium sulfate |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2948592A true US2948592A (en) | 1960-08-09 |
Family
ID=25160407
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US793630A Expired - Lifetime US2948592A (en) | 1959-02-16 | 1959-02-16 | Process for producing pure boric acid and potassium sulfate |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2948592A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3336115A (en) * | 1963-11-21 | 1967-08-15 | American Potash & Chem Corp | Separately crystallizing boric acid and alkali sulfate from aqueous solution by evaporation at different temperatures |
| US3656891A (en) * | 1970-08-05 | 1972-04-18 | Occidental Petroleum Corp | Process for the production of potassium sulfate and borax |
| US4289662A (en) * | 1978-03-31 | 1981-09-15 | Hjh Chemicals, Inc. | Method of making crude boric acid from borate and sulfuric acid |
| CN112158861A (en) * | 2020-05-15 | 2021-01-01 | 青岛碱业钾肥科技有限公司 | Production system of low chlorine potassium sulfate |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1888391A (en) * | 1928-04-16 | 1932-11-22 | Pacific Coast Borax Company | Process of preparing boric acid |
| US2014009A (en) * | 1932-07-25 | 1935-09-10 | Arlyn T Vance | Tympanic pneumo massage device |
| US2637626A (en) * | 1947-07-31 | 1953-05-05 | Borax Cons Ltd | Production and separation of anhydrous alkali metal sulfate and boric acid |
-
1959
- 1959-02-16 US US793630A patent/US2948592A/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1888391A (en) * | 1928-04-16 | 1932-11-22 | Pacific Coast Borax Company | Process of preparing boric acid |
| US2014009A (en) * | 1932-07-25 | 1935-09-10 | Arlyn T Vance | Tympanic pneumo massage device |
| US2637626A (en) * | 1947-07-31 | 1953-05-05 | Borax Cons Ltd | Production and separation of anhydrous alkali metal sulfate and boric acid |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3336115A (en) * | 1963-11-21 | 1967-08-15 | American Potash & Chem Corp | Separately crystallizing boric acid and alkali sulfate from aqueous solution by evaporation at different temperatures |
| US3656891A (en) * | 1970-08-05 | 1972-04-18 | Occidental Petroleum Corp | Process for the production of potassium sulfate and borax |
| US4289662A (en) * | 1978-03-31 | 1981-09-15 | Hjh Chemicals, Inc. | Method of making crude boric acid from borate and sulfuric acid |
| CN112158861A (en) * | 2020-05-15 | 2021-01-01 | 青岛碱业钾肥科技有限公司 | Production system of low chlorine potassium sulfate |
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